Clearance Summary
TRITEC DOC TM received FDA 510(k) clearance under submission number K813075, sponsored by Tri-Tech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1981-12-09.
- Submission: K813075
- Applicant / Sponsor: Tri-Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 1981-12-09
Classification & Regulation
This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.